Canonical Allele Identifier: PA658659840
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 450597
ClinVar RCV Id: RCV000523148

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159435.1:p.Glu1971Gln
CA349063242
NM_001165963.4:c.5911G>C